HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → HCID 14547437, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| Reactant | HCID 22165626 | HCID 22165626 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 14547437 | HCID 14547437 | 83.9% |
Reaction Steps
A solution of 4-{[4-(2,3-dichlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-1,4-dihydropyrid-2-yl]methoxy}-2-butynoic acid (2.50 g), benzyltrimethylammonium hydroxide (0.87 g) and ethyl bromide (0.62 g) in dimethyl sulphoxide (5 ml) was stirred at room temperature for 48 hours, quenched into water and extracted twice into ethyl acetate. The combined ethyl acetate extracts were washed with water, dried over MgSO4 and evaporated. The residue was crystallised from methanol to give the title compound (2.22 g), m.p. 123°-125°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04957930 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-ebd52f2847054a9c9a1feead079515f2 |
| Source note | uspto-grants-1990_09 |